Section 4 - Genetic diversity and adaptation Flashcards
Define mutation
Any change to the quality or the base sequence of the DNA of an organism.
When do mutations occur?
During teh formation of gametes may be inherited, often producing sudden and distinct differences between individuals.
Define gene mutation
Any change to one or more nucleotide bases or a change in the sequence of the bases in DNA
What is substitution mutation?
The type of gene mutation in which a nucleotide in a DNA molecule is replaced by another nucelotide that has a different base.
What is the significance of substitution mutation?
Will depend upon the precise role of the original amino acid.
If it is important in forming bonds that determine the tertiary structure of the final protein, then the replacement amino acid may not form the same bonds.
The protein may then be a different shape and therefore not function properly.
How can the effect of a substitute mutation be different if the new triplet of bases still code for the same amino acid as before?
Due to the degenerate nature of the genetic code, in which most amino acids have more than one codon.
What is a deletion mutation?
A gene mutation by deletion arises when a nucleotide is lost from the normal DNA sequence.
The loss of a single nucleotide from the thousands in a typical gene may seem a minor change but the consequences can be considerable. The amino acid sequence will be entirely different so the polypeptide is unlikely to function correctly.
What is a chromosome mutation?
Changes in the structure or number of whole chromosomes.
What are the two reasons for chromosome mutations?
- changes in whole sets of chromosomes
- changes in the number of individual chromosomes.
How can chromosome mutations occur due to the change in whole sets of chromosomes?
Occur when organisms have three or more sets of chromosomes rather than the usual two.
This is called polyploidy and occurs mostly in plants.
What is polyploidy?
Occur when organisms have three or more sets of chromosomes rather than the usual two.
How can a chromosome mutation occur due to changes in the number of individual chromosomes?
Sometimes individuals homologous pairs of chromosomes fail to separate during meiosis. Known as non-disjunction a usually results in a gamete having either one more or one fewer chromosome.
What is a non-disjunction mutation?
Sometimes individuals homologous pairs of chromosomes fail to separate during meiosis. Known as non-disjunction a usually results in a gamete having either one more or one fewer chromosome.
What two ways does cell division occur?
- Mitosis produces two daughter cells with the same number of chromosomes as the parent cell and as each other
- Meiosis usually produces four daughter cells each with half the number of chromosomes as the parent cell.
What happens during sexual reproduction?
Two gametes fuse to give rise to new offspring.
If each gamete had a full set of chromosomes (diploid number) then the cell that they produce has double this number. - 46 in humans so each cell would have 92.
How are ferns different in terms of reproduction?
Gametes are produced by mitosis. In the fern life cycle, meiosis occurs in the formation of spores.
In more other animals meiosis occurs in the formation of gametes.
What is a haploid number of chromosomes?
During meiosis homologous pairs of chromosomes separate so that only one chromosome from each pair enters a daughter cell.
23 in humans.
When two haploid gametes fuse at fertilisation the diploid number of chromosomes is restored.
What is the process of meiosis?
Two nuclear divisions that normally occur immediately one after the other:
- In the First division meiosis 1 - Homologous chromosomes pair up and their chromatids wrap around each other. Equivalent portions of these chromatids may be exchanged during crossing over. By the end of this division, the homologous pairs have separated, one chromosome from each pair going into one of the two daughter cells.
- Second meiotic division (meiosis 2) - chromatids move apart. At the end, four cells have usually been formed. In humans, each contains 23 chromosomes.
In addition to halving the number of chromosomes what does meiosis produce?
Genetic variation among the offspring, this can lead to adaptations that improve survival chances.
In what two ways does meiosis being about genetic variations?
- Independent segregation of homologous chromosomes
- new combinations of maternal and paternal alleles by crossing over.